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Investigating the Pathogenesis of MYH7 Mutation Gly823Glu in Familial Hypertrophic Cardiomyopathy using a Mouse Model
Published on: August 8, 2022
Facioscapulohumeral muscular dystrophy presenting with hypertrophic cardiomyopathy: a case study
Masahiro Tsuji1, Makoto Kinoshita, Yukihiro Imai
1Department of Pediatrics, Kobe City, Medical Center, General Hospital, 6-4 Nakamachi, Minatojima, Chuo-ku, Kobe 650-0046, Japan. m-tsuji@kcgh.gr.jp
Abstract:
Only three facioscapulohumeral muscular dystrophy (FSHD) patients have been reported to have cardiomyopathy. An asymptomatic 38-year-old man was incidentally found to have electrocardiographic abnormalities. His echocardiogram demonstrated mild dilatation of the left ventricle and poor contractility. Cardiac histopathology indicated hypertrophic cardiomyopathy. Later he developed muscle weakness in the right arm. Scapular winging and asymmetrical facial weakness were evident. Muscle biopsy at the age of 44 years showed myopathic changes consistent with FSHD. His daughter had symptoms of infantile FSHD, which was genetically confirmed. This is the first report of an FSHD patient with biopsy-proven cardiomyopathy.
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